A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741433



Internal ID165099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:91556542..91565000hg38UCSC Ensembl
chrX:90811541..90819999hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg388459
hg198459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426497
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741433
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00272251


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer